Tissue Responses to Endovascular Stent Grafts for Saccular Abdominal Aortic Aneurysms in a Canine Model

We investigated tissue responses to endoskeleton stent grafts for saccular abdominal aortic aneurysms (AAAs) in canines. Saccular AAAs were made with Dacron patch in 8 dogs, and were excluded by endoskeleton stent grafts composed of nitinol stent and expanded polytetrafluoroethylene graft. Animals were sacrificed at 2 months (Group 1; n = 3) or 6 months (Group 2; n = 5) after the placement, respectively. The aortas embedding stent grafts were excised en bloc for gross inspection and sliced at 5 to 8 mm intervals for histopathologic evaluation. Stent grafts were patent in all except a dog showing a thrombotic occlusion in Group 2. In the 7 dogs with patent lumen, the graft overhanging the saccular aneurysm was covered by thick or thin thrombi with no endothelial layer, and the graft over the aortic wall was completely covered by neointima with an endothelial layer. Transgraft cell migration was less active at an aneurysm than at adjacent normal aorta. In conclusion, endoskeleton stent grafts over saccular aneurysms show no endothelial coverage and poor transgraft cell migration in a canine model.

Polytetrafluorethylene added to acrylic resins: mechanical properties

The addition of different polymers, such as polytetrafluorethylene (PTFE), to denture base resins could be an option to modify acrylic resin mechanical properties. This study evaluated the surface hardness, impact and flexural strength, flexural modulus and peak load of 2 acrylic resins, one subjected to a long and another subjected to a short polymerization cycle, which were prepared with or without the addition of 2 percent PTFE. Four groups were formed according to the polymerization cycle and addition or not of PTFE. Forty specimens were prepared for each test (10 per group) with the following dimensions: hardness (30 mm diameter x 5 mm thick), impact strength (50 x 6 x 4 mm) and flexural strength (64 x 10 x 3.3 mm) test. The results of the flexural strength test allowed calculating flexural modulus and peak of load values. All tests were performed in accordance with the ISO 1567:1999 standard. Data were analyzed statistically by ANOVA and Tukey's test with the level of significance set at 5 percent. No statistically significant differences (p>0.05) were found for surface hardness. Flexural strength, impact strength and peak load were significantly higher (p<0.05) for resins without added PTFE. The flexural modulus of the acrylic resin with incorporated 2 percent PTFE polymerized by long cycle was significantly higher (p<0.05) than that of the other resins. Within the limits of this study, it may be concluded that the addition of PTFE did not improve the mechanical properties of the evaluated acrylic resins.

A adição de diferentes polímeros como o politetrafluoretileno (PTFE) às resinas para base de próteses removíveis pode ser uma opção para modificar as propriedades mecânicas das resinas acrílicas. Este estudo avaliou a dureza de superfície, a resistência ao impacto e à flexão, o módulo flexural e a carga de ruptura de duas resinas acrílicas, uma submetida ao ciclo longo e a outra ao ciclo curto de polimerização, as quais foram preparadas com ou sem a adição de PTFE a 2 por cento. Quatro grupos foram formados de acordo com os ciclos de polimerização e a adição ou não de PTFE. Quarenta espécimes foram preparados para cada teste (10 espécimes por grupo) com as seguintes dimensões: dureza de superfície (30 mm diametro x 5 mm espessura), resistência ao impacto (50 x 6 x 4 mm), resistência à flexão (64 x 10 x 3,3 mm). O módulo flexural e a carga de ruptura foram calculados a partir dos valores obtidos no teste de resistência à flexão. Todos os testes foram realizados em conformidade com a Norma ISO 1567:1999. Os dados foram submetidos à análise de variância e teste de Tukey com nível de significância de 5 por cento. Não foram encontradas diferenças estatisticamente significantes (p>0,05) para dureza de superfície. Os valores de resistência à flexão, resistência ao impacto e carga de ruptura foram maiores para as resinas sem a adição de PTFE (p<0,05). O valor do módulo flexural da resina acrílica com adição de PTFE a 2 por cento, polimerizada por ciclo longo, foi maior do que as outras resinas (p<0,05). Dentro das limitações deste estudo, pode-se concluir que a adição de politetrafluoretileno não melhorou as propriedades mecânicas das resinas acrílicas avaliadas.

Evaluation of different sterilization and disinfection methods on commercially made preformed crowns.

The aim of this study was to evaluate the changes caused by different sterilization or disinfection methods on the vestibular surface of four commercially made preformed crowns using stereomicroscopy and scanning electron microscopy (SEM). Preformed crowns (NuSmile Primary Anterior Crown (NSC), Kinder Krowns (KK), Pedo Pearls (PP) and polycarbonate crowns (PC)) were sterilized and/or disinfected by one of the following techniques: no sterilization or disinfection (G1 control group); steam autoclaving at 134 degrees C (30 psi) for 4 min (G2); steam autoclaving at 134 degrees C (30 psi) for 12 min (G3); steam autoclaving at 121 degrees C (15 psi) for 30 min (G4); and ultrasonication in a bath containing 4% Lysetol AF for 5 min at room temperature (chemical disinfection) (G5). Scanning electron micrographs of the crowns were taken before and after their sterilization or disinfection. The changes on the vestibular surface were then scored for the presence or absence of crazing, contour alteration, fracturing, and vestibular surface changes. The data were analyzed statistically using the chi-square test. No changes were observed before and after sterilization or disinfection in the stereomicroscopic evaluation of the vestibular surface of the crowns. However, all methods in which steam autoclaving was used to sterilize the crowns caused significant (P < 0.05) crazing and contour alterations of the vestibular surface of the crowns when they were examined by SEM. Chemical disinfection using an aldehyde-free disinfectant is the preferred method of disinfection for crowns that have been used previously in other dental patients.

Comparative analysis of the shrinkage stress of composite resins

The aim of this study was to compare the shrinkage stress of composite resins by three methods. In the first method, composites were inserted between two stainless steel plates. One of the plates was connected to a 20 kgf load cell of a universal testing machine (EMIC-DL-500). In the second method, disk-shaped cavities were prepared in 2-mm-thick Teflon molds and filled with the different composites. Gaps between the composites and molds formed after polymerization were evaluated microscopically. In the third method, the wall-to-wall shrinkage stress of the resins that were placed in bovine dentin cavities was evaluated. The gaps were measured microscopically. Data were analyzed by one-way ANOVA and Tukey's test (alpha=0.05). The obtained contraction forces were: Grandio = 12.18 ± 0.428N; Filtek Z 250 = 11.80 ± 0.760N; Filtek Supreme = 11.80 ± 0.707 N; and Admira = 11.89 ± 0.647 N. The gaps obtained between composites and Teflon molds were: Filtek Z 250 = 0.51 ± 0.0357 percent; Filtek Supreme = 0.36 ± 0.0438 percent; Admira = 0.25 ± 0.0346 percent and Grandio = 0.16 ± 0.008 percent. The gaps obtained in wall-to-wall contraction were: Filtek Z 250 = 11.33 ± 2.160 µm; Filtek Supreme = 10.66 ± 1.211µm; Admira = 11.16 ± 2.041 µm and Grandio = 10.50 ± 1.224 µm. There were no significant differences among the composite resins obtained with the first (shrinkage stress generated during polymerization) and third method (wall-to-wall shrinkage). The composite resins obtained with the second method (Teflon method) differed significantly regarding gap formation.

Comparison between textured silicone implants and those bonded with expanded polytetrafluoroethylene in rats

PURPOSE: Comparison of the inflammatory reaction promoted by textured silicone implants and that caused by the implant bonded with e-ptfe. METHODS: One-hundred and fifty rats were divided into three equal groups (control, silicone, and bonded e-ptfe). These groups were subdivided into five groups, according to the second operation, i.e., 7,30,60,90 and 180 days. Histology of the peri-implant tissue was analyzed by morphometry with blood count (neutrophilos, lymphocytes, macrophages, fibroblasts and capillaries). RESULTS: Comparison of subgroups 7,30,60,90, 180 days: - neutrophils: silicone: > in subgroup 7 days; bonded e-ptfe: > in subgroups 7 and 30 days; - lymphocytes: silicone: > in subgroup 7 and 180 days; bonded e-ptfe: > in subgroup 180 days; - macrophages: silicone: > in subgroup 7 and 60 days; bonded e-ptfe: > in subgroup 7,30 and 60 days; - fibroblasts: silicone: > in subgroup 30 and 60 days;- vascular volume: silicone: in subgroup 7, 60 and 90 days; bonded e-ptfe: > in subgroup 7 days. Comparison of groups: neutrophils : 7 days: > in silicone and bonded e-ptfe; 30 days: > in bonded e-ptfe; - lymphocytes: - 7,30,90 and 180 days: in the control; macrophages: - 7,30 and 60 days: > in silicone & bonded e-ptfe; 180 days > in silicone; fibroblasts: - 7,30 and 90 days: > in silicone and bonded e-ptfe; 180 days: > in bonded e-ptfe; vascular volume 7,60,90 and 180 days: > in silicone and bonded e-ptfe; 30 days: > in bonded e-ptfe. CONCLUSIONS: The acute stage of the inflammatory response was more severe and irregular in the silicone implant; both the silicone implant and the silicone bonded with e-ptfe promoted chronic inflammatory reaction and weak foreign body inflammatory response. These reactions were greater in the silicone implant group.

OBJETIVO: Comparar a reação inflamatória provocada pelo implante de silicone texturizado, com aquela causada por este recoberto com PTFE-E. MÉTODOS: Foram utilizadas 150 ratas, divididos em três grupos igruais (controle, silicone e recoberto PTFE-E). Os grupos foram subdivididos em cinco subgrupos, ou seja, 7, 30, 60, 90 e 180 dias, de acordo com a data do segundo ato operatório. O tecido perimplante foi analisado histologicamente, por meio de técnica morfométrica, com contagem de neutrófilos, linfócitos, macrófagos, fibroblastos e capilares. RESULTADOS: Comparação dos subgrupos 7, 30, 60, 90 180 dias: - neutrófilos - silicone: > no subgrupo 7 dias; rec-ptfe: > nos subgrupos 7 e 30 dias; - linfócitos: silicone: > no subgrupo 7 e 180 dias; rec-ptfe: > no subgrupo 180 dias; - macrófagos: silicone: > no subgrupo 7 e 60 dias; rec-ptfe: > no subgrupo 7, 30 e 60 dias; - fibroblastos: silicone: > no subgrupo 30 e 60 dias; - volume vascular: silicone: > no subrupo 7, 60 e 90 dias; rec-ptfe: > no subgrupo 7 dias . Comparação dos gurpos: - neutrófilos - 7 dias: > no silicone e rec-ptfe; 30 dias: > no rec-ptfe; - linfócitos - 7, 30, 90 e 180 dias: > no controle; - macrófagos - 7, 30 e 60 dias: > no silcone e rec-ptfe; 180 dias: > no silicone; - fibroblastos - 7, 30 e 90 dias: > no silicone e rec-ptfe; 180 dias: > no rec-ptfe; - volume vascular - 7, 60, 90 e 180 dias: > no silicone e rec-ptfe; 30 dias: > no rec-ptfe. CONCLUSÕES: A fase aguda da reação inflamatória foi mais intensa e irregular no implante de silicone; tanto o implante de silicone como o de silicone recoberto por ptfe-e induziram a reação inflamatória crônica e a fraca reação inflamatória tipo corpo estranho. Estas forram maiores no implante de silicone.

Textile anionic dyes recovery using tri-n-butyl phosphate as carrier through supported liquid membrane.

The recovery of anionic dyes Acid Red10 B (CI Acid Violet 54) and Acid Pink BE (CI Acid Red 183) in flat type supported liquid membrane (SLM) using tri-n-butyl phosphate as carrier was studied. The parameters studied were the effect of feed phase pH, stripping reagent concentration, string speed and initial dye concentration on permeability of dyes. The influence of salt concentration such as sodium chloride and sodium sulphate on the dye recovery was examined. The reusability of membrane and kinetics of transport were also studied. The optimum conditions of transport are feed phase pH 1 +/- 0.1, 0.1 M sodium hydroxide as stripping phase, stirring speed at 500 rpm. The maximum recovery under optimum conditions was observed as 94.2 % for Acid Red10 B and 85.7 % for Acid Pink BE. The maximum permeability was 11.0 x 10(-6) m/s for Acid Red10 B and 7.7 x 10(-6) m/s for Acid Pink BE.

Surgarcane biopolymer patch in femoral artery angioplasty on dogs

PURPOSE: The objective of this study was to evaluate the use of the sugarcane biopolymer membrane in femoral artery patch angioplasty on dogs. METHODS: Eight dogs were submitted to bilateral femoral artery patch angioplasty with a sugarcane biopolymer membrane patch on one side and e-PTFE patch on the contralateral side. This research was performed at Experimental Surgical Research Laboratory of the Centro de Ciências da Saúde at Universidade Federal de Pernambuco. The dogs were submitted to a new surgery at 180 days after the patch angioplasty in order to harvest the femoral artery. All the animals were evaluated by: clinical examination, measure of femoral artery diameter, arteriogram and Doppler fluxometry. Yet the material harvested was sent to histological study. Each animal served as its own control. RESULTS: In all vessels of both groups there were no cases of infection, aneurysm formation, rupture or pseudoaneurysm formation and thrombosis. In both groups it was observed a chronic inflammatory reaction with lymphocytes, neutrophils and fibrosis in the outer surface of the patches. It was observed fibrosis in the inner surfaces of all the patches. In e-PTFE patches occurred invasion by fibroblasts. CONCLUSION: The sugarcane biopolymer membrane can be used as a patch in femoral artery angioplasty on dogs.

OBJETIVO: Avaliar a utilização da membrana do biopolímero de cana-de-açúcar quando utilizada como remendo em arterioplastias femorais de cães. MÉTODOS: Oito cães foram submetidos a arterioplastia femoral bilateral com enxertos em remendo com a membrana do biopolímero de cana-de-açúcar em um lado e com a prótese de e-PTFE no lado contra-lateral. Os experimentos foram realizados no Núcleo de Cirurgia Experimental do Centro de Ciências da Saúde da Universidade Federal de Pernambuco. A avaliação dos animais foi realizada através do exame clínico, da medida do diâmetro das artérias femorais, da fluxometria Doppler, da arteriografia e da histologia. Após 180 dias os cães foram submetidos a nova cirurgia para retirada dos segmentos das artérias femorais com os implantes. RESULTADOS: No período de avaliação nos dois grupos, não se observou casos de infecção, dilatação, ruptura ou falso-aneurisma e trombose. Nos dois grupos foi encontrada uma resposta inflamatória crônica com neutrófilos, linfócitos e fibrose na superfície externa dos remendos. Foi observada também a presença de fibrose na superfície interna em ambos os grupos. No grupo controle ocorreu invasão dos remendos de e-PTFE por fibroblastos. CONCLUSÃO: A membrana do biopolímero de cana-de-açúcar pode ser utilizada como remendo em arterioplastias femorais de cães.

Regeneración ósea guiada de cara al año 2000. Consideraciones clínicas y biológicas / Guided bone regeneration facing the year 2000. Clinical and biologic considerations

La regeneración ósea guiada representa hoy una de las terapias de mayor éxito para el manejo conjunto a la colocación de implantes. Durante los últimos años el uso de membranas para la regeneración ósea ha ido combinada desde membranas no reabsorbibles hasta membranas reabsorbibles. El presente artículo pretende mostrar a fondo los diferentes tipos de membranas que se tienen en el mercado, así como los resultados mostrados con el uso de las mismas. Asimismo, se hace un ligero repaso de las indicaciones para la regeneración ósea guiada y las propiedades que debe tener una membrana para poder ser utilizada en la regeneración ósea guiada

Nuevos enfoques en cirugía perirradicular: revisión de la literatura / New approaches in periradicular surgery: review of the literature

Cuando se genera una lesión periapical como consecuencia de un proceso inflamatorio crónico y posterior necrosis pulpar, se hace necesaria una terapia encaminada a eliminar el agente etiológico primario, lo que frecuentemente se resuelve exitosamente con un tratamiento endodóntico convencional. Sin embargo, en algunas casos persiste un estado inflamatorio manifestándose una patología periapical, que puede ser un granuloma o quiste perirradicular con o sin presencia de tractos sinuosos. Cuando la infección no puede ser erradicada por vía ortógrada, está indicada una cirugía endodóntica. La regeneración del defecto óseo periapical a veces no se da debido a migración del epitelio bucal o del tejido conjuntivo gingival hacia el defecto óseo, evitando la formación de hueso trabecular normal y haciendo necesarias nuevas cirugías de reentrada. La literatura reporta recientes materiales de obturación radicular terminal y elementos de regeneración tisular guiada para mejorar la predecibilidad del tratamiento quirúrgico. Sustituyendo la amalgama como material convencional de relleno transapical se encuentran actualmente los nuevos materiales derivados del óxido de zinc y eugenol (IRM y Super EBA) y últimamente el MTA o agregado de trióxidos minerales y como materiales de RTG se encuentran membranas bioabsorbibles, materiales sustitutos de hueso (hidroxiapatitas, hueso liofilizado) e injertos de periostio autólogo libres y pediculados